NDC11 70742028200

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDC	Product root
70742-0282-0	70742-0282
70742-0282-00	70742-0282
70742-282-00	70742-282

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
BODY ACTION PRODUCTS Climax Control Gel	BENZOCAINE	PRODUCT MAX GROUP INC	53e746cc-0078-4381-bf0b-9c8f98d66904	2023-11-10	Warnings	Exact identifier ndc (package): 70742-282-00 ndc (product): 70742-282 ndc11 (package): 70742028200

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.